Good and bad news for Human Genome Sciences, as it files Benlysta BLA but mapatumumab disappoints in Ph II

11 June 2010

There was mixed news for Maryland-USA-based Human Genome Sciences this week, with the fling ahead of expectations of a Biologics License Application to the US Food and Drug Administration for approval to market Benlysta (belimumab) for the treatment of systemic lupus erythematosus (SLE) but also negative results from a mid-stage study of its advanced multiple myeloma drug candidate mapatumumab.

HGS announced the results of its randomized Phase II trial of mapatumumab (HGS-ETR1) in combination with bortezomib (Velcade) in patients with advanced multiple myeloma.

The results demonstrated no difference in disease response or progression-free survival for the combination that included mapatumumab versus the control group receiving bortezomib alone, but showed that mapatumumab was well tolerated in this study. HGS said it expects to report full results from the trial at a scientific meeting later in 2010.

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